Treatment of short bowel syndrome patients with colon-in-continuity

Abstract

Intestinal absorption is enhanced in short bowel syndrome patients presenting with colon-in-continuity by treatment with a GLP-2 receptor agonist, such as teduglutide.

We claim: 
     
       1. A method of treating an adult human patient having short bowel syndrome secondary to Crohn's disease, who receives parenteral nutrition each week, and who presents with colon-in-continuity with remnant small intestine, said method comprising administering [Gly2]hGLP-2 to said patient using a dosing regimen effective to reduce or eliminate said weekly parenteral nutrition received by said patient. 
     
     
       2. The method of  claim 1 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 5 to 500 μg/kg. 
     
     
       3. The method of  claim 2 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 30 to 150 μg/kg. 
     
     
       4. The method of  claim 1 , wherein the [Gly2]hGLP-2 is administered by subcutaneous injection. 
     
     
       5. The method of  claim 4 , wherein the subcutaneous injection is into the abdomen, thigh, or arm. 
     
     
       6. A method of treating an adult human patient having short bowel syndrome secondary to Crohn's disease, who receives parenteral nutrition each week, and who presents with colon-in-continuity with remnant small intestine, said method comprising administering [Gly2]hGLP-2 to said patient using a dosing regimen effective to increase wet weight absorption compared to a baseline wet weight absorption by said patient. 
     
     
       7. The method of  claim 6 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 5 to 500 μg/kg. 
     
     
       8. The method of  claim 7 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 30 to 150 μg/kg. 
     
     
       9. The method of  claim 6 , wherein the [Gly2]hGLP-2 is administered by subcutaneous injection. 
     
     
       10. The method of  claim 9 , wherein the subcutaneous injection is into the abdomen, thigh, or arm. 
     
     
       11. The method of  claim 1 , wherein said regimen comprises administration of said [Gly2]hGLP-2 over a period of at least 21 days. 
     
     
       12. The method of  claim 6 , wherein said regimen comprises administration of said [Gly2]hGLP-2 over a period of at least 21 days. 
     
     
       13. The method of  claim 1 , wherein the parenteral nutrition is reduced by volume or frequency of administration. 
     
     
       14. The method of  claim 1 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 30 to 150 μg/kg by subcutaneous injection. 
     
     
       15. The method of  claim 6 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 30 to 150 μg/kg by subcutaneous injection.